| 2008 | Selective A3 adenosine receptor antagonists derived from nucleosides containing a bicyclo[3.1.0]hexane ring system | 정낙신 | Article |
| 2005 | Short synthesis of L-ribose and its utility to L-fluoro-neplanocin A | 정낙신 | Meeting Abstract |
| 2011 | Stereoselective amination of chiral benzylic ethers using chlorosulfonyl isocyanate: Total synthesis of (+)-Sertraline | 정낙신 | Article |
| 2006 | Stereoselective functionalization of the 1′-position of 4′-thionucleosides | 정낙신; 최선; 류재상 | Article |
| 2010 | Stereoselective Synthesis and Anti-HCV Activity of 2΄-C-Substituted Cyclopropyl-Fused Carbanucleosides | 고윤정 | Master's Thesis |
| 2012 | Stereoselective synthesis and anti-HCV activity of conformationally restricted 2′-C-substituted carbanucleosides | 정낙신; 최원준 | Article |
| 2008 | Stereoselective synthesis and conformational study of novel 2′,3′-didehydro-2′,3′-dideoxy-4′-selenonucleosides | 정낙신; 최선; 최원준 | Article |
| 2007 | Stereoselective synthesis of 1 '-subtituted-4 '-thionucleosides | 정낙신 | Meeting Abstract |
| 2007 | Stereoselective synthesis of 1′-functionalized-4′- thionucleosides | 정낙신 | Article |
| 2006 | Stereoselective synthesis of 2′-C-methyl-cyclopropyl-fused carbanucleosides as potential anti-HCV agents | 정낙신 | Article |
| 2011 | Stereoselective Synthesis of 2′-Deoxy-2′-fluoro-4′-selenoarabinofuranosyl Pyrimidines as Potent Anticancer Agents | 유진하 | Master's Thesis |
| 2005 | Stereoselective synthesis of 3-hydroxymethyl-D-cyclopentenone, the versatile intermediate for the synthesis of carbocyclic nucleosides | 이강만; 신윤용; 정낙신 | Conference Paper |
| 2011 | Stereoselective Synthesis of 4'-Selenopurine Nucleosides as Potential A3 Adenosine Receptor Ligands | 이한길 | Master's Thesis |
| 2002 | Stereoselective synthesis of a novel apio analogue of neplanocin A as potential S-adenosylhomocysteine hydrolase inhibitor | 이강만; 정낙신 | Article |
| 2002 | Stereoselective synthesis of amino-substituted apio dideoxynucleosides through a distant neighboring group effect | 정낙신 | Article |
| 2005 | Stereoselective synthesis of conformationally rigid apio carbanucleosides as potential antiviral agents | 정낙신 | Conference Paper |
| 2012 | Stereoselective Synthesis of Fluoro-homoneplanocin A as a Potential Antiviral Agent | 이지예 | Master's Thesis |
| 2012 | Stereoselective synthesis of fluoro-homoneplanocin A as a potential antiviral agent | 정낙신 | Article |
| 2007 | Stereoselective synthesis of homo-apioneplanocin A as potential inhibitor of S-adenosylhomocysteine hydrolase | 이강만; 정낙신 | Conference Paper |
| 2011 | Stereoselective synthesis of MLN4924, an inhibitor of NEDD8-activating enzyme | 정낙신; 최원준 | Article |
| 2005 | Stereoselective synthesis of novel thioiso dideoxy nucleosides with exocyclic methylene as potential antiviral agents | 정낙신 | Conference Paper |
| 2004 | Structural determinants of efficacy at A3 adenosine receptors: Modification of the ribose moiety | 정낙신 | Article |
| 2011 | Structural studies of S-Adenosylhomocysteine hydrolase and binding mode analysis with novel mechanism-based inhibitors, halo-neplanocin A analogs | 정낙신; 최선 | Meeting Abstract |
| 2000 | Structural study of antisense dimers, modified adenosine-thymidine phosphorothioate | 정낙신 | Article |
| 2005 | Structure-activity relationship of 5′-substituted fluoro-neplanocin A analogues as potent inhibitors of S-adenosylhomocysteine hydrolase | 이강만; 정낙신; 이상국 | Conference Paper |
| 2004 | Structure-activity relationship of N6-substituted D-4 '-thioadenosine derivatives as potent and selective agonists at the human A3 adenosine receptor. | 정낙신 | Meeting Abstract |
| 2007 | Structure-activity relationships of 2-chloro-N-6-substituted-4 '-thioadenosine-5 ''-dialkylamides as potent and selective human A(3) adenosine receptor antagonists | 정낙신 | Meeting Abstract |
| 2006 | Structure-activity relationships of 2-chloro-N6-substituted- 4′-thioadenosine-5′-uronamides as highly potent and selective agonists at the human A3 adenosine receptor | 정낙신; 이상국 | Article |
| 2005 | Structure-activity relationships of 2-chloro-N6-substituted-4'-thioadenosine-5'-uronamides as human A3 adenosine receptor agonists | 정낙신; 이상국 | Meeting Abstract |
| 2008 | Structure-activity relationships of 2-chloro-N6-substituted-4′-thioadenosine-5′-N,N-dialkyluronamides as human A3 adenosine receptor antagonists | 정낙신; 최원준 | Article |
